Canonical Allele Identifier: CA370199464
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660734T>G , CM000669.2:g.152660734T>G GRCh38
NC_000007.13:g.152357819T>G , CM000669.1:g.152357819T>G GRCh37
NC_000007.12:g.151988752T>G NCBI36
NG_027988.1:g.20432A>C
NG_027988.2:g.20432A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11371A>C ENSP00000513758.1:n.-47-11371A>C
ENST00000698507.1:n.156A>C
ENST00000359321.2:c.88A>C MANE Select ENSP00000352271.1:p.Asn30His
ENST00000359321.1:c.88A>C ENSP00000352271.1:p.Asn30His
ENST00000495707.1:n.110A>C
NM_005431.1:c.88A>C NP_005422.1:p.Asn30His
NM_005431.2:c.88A>C MANE Select NP_005422.1:p.Asn30His